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Multicomponent Synthesis of 4-unsubstituted 5-nitropyridine Derivatives Научная публикация

Журнал Synthetic Communications
ISSN: 0039-7911 , E-ISSN: 1532-2432
Вых. Данные Год: 2020, Том: 50, Номер: 16, Страницы: 2432-2439 Страниц : 9 DOI: 10.1080/00397911.2020.1780261
Ключевые слова Green chemistry, 5-nitro-1,4-dihydropyridines, 5-nitropyridines, multicomponent reaction
Авторы Kulakov Ivan V. 1 , Oleshchuk Alena L. 1,2 , Koveza Vladislav A. 2 , Palamarchuk Irina V. 1
Организации
1 Institute of Chemistry, Tyumen State University
2 Faculty of Chemistry, Omsk F. M. Dostoevsky State University

Реферат: Multicomponent reaction of 2-nitroacetophenone, urotropine (or paraformaldehyde), β-dicarbonyl compound and ammonium acetate afforded five new 4-unsubstituted 5-nitro-6-phenyl-1,4-dihydropyridine derivatives, oxidation of which provided the corresponding 5-nitro-6-phenylpyridines. The proposed approach for the synthesis of 4-unsubstituted 5-nitro-6-phenyl-1,4-dihydropyridines and their subsequent aromatization into pyridines made it possible to reduce the total reaction time by more than 200 times and the overall yield of 5-nitro-6-phenylpyridine by 2 times compared with the known methods.
Библиографическая ссылка: Kulakov I.V. , Oleshchuk A.L. , Koveza V.A. , Palamarchuk I.V.
Multicomponent Synthesis of 4-unsubstituted 5-nitropyridine Derivatives
Synthetic Communications. 2020. V.50. N16. P.2432-2439. DOI: 10.1080/00397911.2020.1780261 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 22 дек. 2019 г.
Опубликована online: 23 июн. 2020 г.
Опубликована в печати: 17 авг. 2020 г.
Идентификаторы БД:
Web of science: WOS:000547312400001
Scopus: 2-s2.0-85087375165
РИНЦ: 45496904
Chemical Abstracts: 2020:2055297
Chemical Abstracts (print): 173:817773
OpenAlex: W3036963612
Цитирование в БД:
БД Цитирований
Web of science 8
Scopus 8
OpenAlex 9
Альметрики: